PMID- 25504156 OWN - NLM STAT- MEDLINE DCOM- 20160318 LR - 20220317 IS - 1865-8652 (Electronic) IS - 0741-238X (Print) IS - 0741-238X (Linking) VI - 31 IP - 12 DP - 2014 Dec TI - Retrospective analysis of long-term adherence to and persistence with DPP-4 inhibitors in US adults with type 2 diabetes mellitus. PG - 1287-305 LID - 10.1007/s12325-014-0171-3 [doi] AB - INTRODUCTION: Patients with type 2 diabetes mellitus (T2DM) must remain adherent and persistent on antidiabetic medications to optimize clinical benefits. This analysis compared adherence and persistence among adults initiating dipeptidyl peptidase-4 inhibitors (DPP-4is), sulfonylureas (SUs), and thiazolidinediones (TZDs) and between patients initiating saxagliptin or sitagliptin, two DPP-4is. METHODS: This retrospective cohort study utilized the US MarketScan((R)) (Truven Health Analytics, Ann Arbor, MI, USA) Commercial and Medicare Supplemental health insurance claims databases. Adults aged >/=18 years with T2DM who initiated a DPP-4i, SU, or TZD from January 1, 2009 to January 31, 2012 were included. Patients must have been continuously enrolled for >/=1 year prior to and >/=1 year following initiation. Adherence was measured using proportion of days covered (PDC), with PDC >/= 0.80 considered adherent. Persistence was measured as time to discontinuation, defined as last day with drug prior to a 60+ days gap in therapy. Multivariable logistic regression and Cox proportional hazards models compared the outcomes between cohorts, controlling for baseline differences. RESULTS: The sample included 238,372 patients (61,399 DPP-4i, 134,961 SU, 42,012 TZD). During 1-year follow-up, 47.3% of DPP-4i initiators, 41.2% of SU initiators, and 36.7% of TZD initiators were adherent. Adjusted odds of adherence were significantly greater among DPP-4i initiators than SU (adjusted odds ratio [AOR] = 1.678, P < 0.001) and TZD initiators (AOR = 1.605, P < 0.001). During 1-year follow-up, 55.0% of DPP-4i initiators, 47.8% of SU initiators, and 42.9% of TZD initiators did not discontinue therapy. Adjusted hazards of discontinuation were significantly greater for SU (adjusted hazard ratio [AHR] = 1.390, P < 0.001) and TZD initiators (AHR = 1.402, P < 0.001) compared with DPP-4i initiators. Saxagliptin initiators had significantly better adherence (AOR = 1.213, P < 0.001) compared with sitagliptin initiators, and sitagliptin initiators had significantly greater hazard of discontinuation (AHR = 1.159, P < 0.001). Results were similar over a 2-year follow-up. CONCLUSIONS: US adults with T2DM who initiated DPP-4i therapy, particularly saxagliptin, had significantly better adherence and persistence compared with patients who initiated SUs or TZDs. FAU - Farr, Amanda M AU - Farr AM AD - Truven Health Analytics, 7700 Old Georgetown Road, 6th Floor, Bethesda, MD, 20814, USA, amanda.farr@truvenhealth.com. FAU - Sheehan, John J AU - Sheehan JJ FAU - Curkendall, Suellen M AU - Curkendall SM FAU - Smith, David M AU - Smith DM FAU - Johnston, Stephen S AU - Johnston SS FAU - Kalsekar, Iftekhar AU - Kalsekar I LA - eng PT - Journal Article PT - Observational Study PT - Research Support, Non-U.S. Gov't DEP - 20141212 PL - United States TA - Adv Ther JT - Advances in therapy JID - 8611864 RN - 0 (Dipeptides) RN - 0 (Dipeptidyl-Peptidase IV Inhibitors) RN - 0 (Hypoglycemic Agents) RN - 0 (Sulfonylurea Compounds) RN - 9GB927LAJW (saxagliptin) RN - PJY633525U (Adamantane) RN - TS63EW8X6F (Sitagliptin Phosphate) MH - Adamantane/*analogs & derivatives/therapeutic use MH - Adult MH - Aged MH - Cohort Studies MH - *Diabetes Mellitus, Type 2/drug therapy/epidemiology MH - Dipeptides/*therapeutic use MH - Dipeptidyl-Peptidase IV Inhibitors/therapeutic use MH - Female MH - Humans MH - Hypoglycemic Agents/therapeutic use MH - Logistic Models MH - Long-Term Care/statistics & numerical data MH - Male MH - Medicare/statistics & numerical data MH - Medication Adherence/*statistics & numerical data MH - Middle Aged MH - Proportional Hazards Models MH - Retrospective Studies MH - Sitagliptin Phosphate/*therapeutic use MH - Sulfonylurea Compounds/*therapeutic use MH - United States/epidemiology PMC - PMC4271133 EDAT- 2014/12/17 06:00 MHDA- 2016/03/19 06:00 PMCR- 2014/12/12 CRDT- 2014/12/16 06:00 PHST- 2014/10/23 00:00 [received] PHST- 2014/12/16 06:00 [entrez] PHST- 2014/12/17 06:00 [pubmed] PHST- 2016/03/19 06:00 [medline] PHST- 2014/12/12 00:00 [pmc-release] AID - 171 [pii] AID - 10.1007/s12325-014-0171-3 [doi] PST - ppublish SO - Adv Ther. 2014 Dec;31(12):1287-305. doi: 10.1007/s12325-014-0171-3. Epub 2014 Dec 12.